| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25626811-25627052 | Common:1; Rare:39 | ||||
| chr3:30607215-30607353 | Rare:34 | ||||
| chr3:30630004-30630068 | Rare:11 | ||||
| chr3:30689091-30689126 | Rare:6 | ||||
| chr3:32239658-32239702 | Rare:8 | ||||
| chr3:32464440-32464649 | Common:5; Rare:54 | ||||
| chr3:32469208-32469281 | Common:1; Rare:13 | ||||
| chr3:32470681-32470998 | Common:5; Rare:45 | ||||
| chr3:32491699-32492041 | Common:4; Rare:62 | ||||
| chr3:37047306-37047573 | Common:2; Rare:59; Clinvar:9; Clinvar (benign):5 | ||||
| chr3:37054413-37054713 | Common:3; Rare:64 | ||||
| chr3:38127813-38127940 | Rare:36 | ||||
| chr3:38455450-38455753 | Common:4; Rare:75 | ||||
| chr3:40453163-40453417 | Common:6; Rare:56 | ||||
| chr3:41203892-41204094 | Rare:31 |